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线粒体相关内质网膜的组成、功能及其在运动预处理心脏保护中的作用

Compositions and Functions of Mitochondria-Associated Endoplasmic Reticulum Membranes and Their Contribution to Cardioprotection by Exercise Preconditioning.

作者信息

Lv Yuhu, Cheng Lin, Peng Fenglin

机构信息

College of Physical Education and Health, Guangxi Normal University, Guilin, China.

出版信息

Front Physiol. 2022 Jun 6;13:910452. doi: 10.3389/fphys.2022.910452. eCollection 2022.

Abstract

Mitochondria-associated endoplasmic reticulum membranes (MAMs) are important components of intracellular signaling and contribute to the regulation of intracellular Ca/lipid homeostasis, mitochondrial dynamics, autophagy/mitophagy, apoptosis, and inflammation. Multiple studies have shown that proteins located on MAMs mediate cardioprotection. Exercise preconditioning (EP) has been shown to protect the myocardium from adverse stimuli, but these mechanisms are still being explored. Recently, a growing body of evidence points to MAMs, suggesting that exercise or EP may be involved in cardioprotection by modulating proteins on MAMs and subsequently affecting MAMs. In this review, we summarize the latest findings on MAMs, analyzing the structure and function of MAMs and the role of MAM-related proteins in cardioprotection. We focused on the possible mechanisms by which exercise or EP can modulate the involvement of MAMs in cardioprotection. We found that EP may affect MAMs by regulating changes in MFN2, MFN1, AMPK, FUNDC1, BECN1, VDAC1, GRP75, IP3R, CYPD, GSK3β, AKT, NLRP3, GRP78, and LC3, thus playing a cardioprotective role. We also provided direction for future studies that may be of interest so that more in-depth studies can be conducted to elucidate the relationship between EP and cardioprotection.

摘要

线粒体相关内质网膜(MAMs)是细胞内信号传导的重要组成部分,有助于调节细胞内钙/脂质稳态、线粒体动力学、自噬/线粒体自噬、细胞凋亡和炎症。多项研究表明,位于MAMs上的蛋白质介导心脏保护作用。运动预处理(EP)已被证明可保护心肌免受不良刺激,但其机制仍在探索中。最近,越来越多的证据指向MAMs,表明运动或EP可能通过调节MAMs上的蛋白质并随后影响MAMs参与心脏保护。在这篇综述中,我们总结了关于MAMs的最新发现,分析了MAMs的结构和功能以及MAM相关蛋白在心脏保护中的作用。我们重点关注运动或EP调节MAMs参与心脏保护的可能机制。我们发现,EP可能通过调节MFN2、MFN1、AMPK、FUNDC1、BECN1、VDAC1、GRP75、IP3R、CYPD、GSK3β、AKT、NLRP3、GRP78和LC3的变化来影响MAMs,从而发挥心脏保护作用。我们还为未来可能感兴趣的研究提供了方向,以便能够进行更深入的研究来阐明EP与心脏保护之间的关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a428/9207531/621825e6b67a/fphys-13-910452-g001.jpg

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